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PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR Adverse Event — Injury (MDR 3006705815-2020-01726)

PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR Adverse Event — Injury (MDR 3006705815-2020-01726) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR; Generic name: SCS IPG; Manufacturer: ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, L

DevicePROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR
Generic nameSCS IPG
ManufacturerST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)
Report number3006705815-2020-01726
Event typeInjury
Product problemN
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, CONSUM
NarrativeTHE RESULTS OF THE INVESTIGATION ARE INCONCLUSIVE SINCE THE DEVICE WAS NOT RETURNED FOR ANALYSIS. BASED ON THE INFORMATION RECEIVED, THE CAUSE OF THE REPORTED INCIDENT COULD NOT BE CONCLUSIVELY DETERMINED.
SourceopenFDA MAUDE (device adverse events)

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